An improved cryo-FIB method for fabrication of frozen hydrated lamella

J Struct Biol. 2016 May;194(2):218-23. doi: 10.1016/j.jsb.2016.02.013. Epub 2016 Feb 12.

Abstract

Cryo-electron tomography (cryo-ET) provides great insights into the ultrastructure of cells and tissues in their native state and provides a promising way to study the in situ 3D structures of macromolecular complexes. However, this technique has been limited on the very thin specimen, which is not applicable for most cells and tissues. Besides cryo-sectioning approach, cryo focused ion beam (cryo-FIB) appeared recently to achieve 'artifact-free' thin frozen hydrated lamella via fabrication. Considering that the current cryo-FIB methods need modified holders or cartridges, here, with a "D-shaped" molybdenum grid and a specific shutter system, we developed a simple cryo-FIB approach for thin frozen hydrated lamella fabrication, which fits both standard transmission cryo-electron microscopes with side-entry cryo-holders and state-of-the-art ones with AutoGrids. Our approach will expand the usage of cryo-FIB approach in many labs.

Keywords: Cell ultrastructure; Cryo-electron tomography; Cryo-focused ion beam; Frozen hydrated lamella; Molybdenum grid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Ascaris suum / cytology
  • Cryoelectron Microscopy / instrumentation
  • Cryoelectron Microscopy / methods*
  • Electron Microscope Tomography / instrumentation
  • Electron Microscope Tomography / methods*
  • Escherichia coli / ultrastructure
  • Fibroblasts / ultrastructure
  • Frozen Sections / methods*
  • Male
  • Mice
  • Sf9 Cells / ultrastructure
  • Spermatozoa / ultrastructure
  • Spodoptera / cytology